Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 52
... protein to direct synthesis . The recent work on the chemical synthesis of insulin [ 27 ] postdates Sanger's meticulous chemical description of this protein . Modern techniques in resolving the primary structure of proteins should lead ...
... protein to direct synthesis . The recent work on the chemical synthesis of insulin [ 27 ] postdates Sanger's meticulous chemical description of this protein . Modern techniques in resolving the primary structure of proteins should lead ...
Seite 65
them , little is known about structural variation in the proteins . Some proteins are known to be deficient in more ... protein . The alteration of the behavior of pseudocholinesterase toward inhibitors is basic enough to identify all ...
them , little is known about structural variation in the proteins . Some proteins are known to be deficient in more ... protein . The alteration of the behavior of pseudocholinesterase toward inhibitors is basic enough to identify all ...
Seite 218
nitely protein . The precise structural basis for these antigenic differences is not yet defined , but it is clear that they result from differences in amino - acid sequence [ lino , 1965 ; Jones & Beale , 1963 ] . Immunochemical ...
nitely protein . The precise structural basis for these antigenic differences is not yet defined , but it is clear that they result from differences in amino - acid sequence [ lino , 1965 ; Jones & Beale , 1963 ] . Immunochemical ...
Inhalt
Welcoming Address | 3 |
Remarks of the Secretary of the Permanent Committee for the International | 11 |
Diagnosis in medical genetics | 29 |
Urheberrecht | |
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abnormal acatalasia acatalatic acid Acta activity alleles Amer amino-acid amino-acid sequence analysis aneuploidy anomalies antibodies antigenic autosomal dominant autosomal recessive biochemical birth blood blood-group catalase cent child chromosome aberrations clinical colonies congenital consanguinity Cytogenetics defect deficiency Dept determined disaccharidases disease distribution duplication effects enzyme evolution factors female gamma globulin gene frequencies hemoglobin heredity is autosomal heterochromatin heterozygotes heterozygous Hospital Human Genetics inactivation individuals inheritance intestinal karyotype L-leut lactase Lancet leukemia linkage loci locus male malformations maltase marker marriage mating Medical mental metabolism Michigan Mongolism mosaic mutation normal observed pairs parents patients pattern pedigree peptide chains Ph¹ phenotype population possible Proc protein recombination records red cells selection sex chromatin sex-linked specific structure studies substance sucrase syndrome synthesis Table techniques tion tissue traits translocation trisomy University variable variation X-chromosome York